rs2834317

GWAS Catalog Trait Associations (8)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

hematocrit

Allele A
OR 0.03
p 9.0e-57
N 928,679
Large GWAS
multi-ancestry
Allele A
OR 0.04
p 2.0e-46
N 562,259
Large GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.02
p 9.0e-21
N 503,490
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.04
p 1.0e-19
N 408,112
Large GWAS
European

hemoglobin measurement

Allele A
OR 0.03
p 2.0e-53
N 928,679
Large GWAS
multi-ancestry
Allele A
OR
p 2.0e-42
N 746,431
Large GWAS
multi-ancestry
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.03
p 2.0e-13
N 584,668
Major Consortium StudyLarge GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.02
p 1.0e-9
N 408,112
Large GWAS
European
Allele A
OR 0.03
p 3.0e-34
N 394,642
Large GWAS
European

serum creatinine amount

Allele A
OR 0.03
p 9.0e-43
N 928,679
Large GWAS
multi-ancestry
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.03
p 2.0e-13
N 600,139
Major Consortium StudyLarge GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.03
p 1.0e-27
N 494,370
Large GWAS
multi-ancestry
Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 6.0e-14
N 450,015
Large GWAS
multi-ancestry
Allele A
OR 0.02
p 2.0e-28
N 394,642
Large GWAS
European

high density lipoprotein cholesterol measurement

Allele A
OR 0.03
p 8.0e-36
N 394,642
Large GWAS
European

glomerular filtration rate

Allele A
OR 0.00
p 3.0e-22
N 1,004,040
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.03
p 3.0e-12
N 571,230
Major Consortium StudyLarge GWAS
multi-ancestry
Allele A
OR 0.00
p 1.0e-14
N 567,460
Large GWAS
European
Allele A
OR 5.65
p 2.0e-8
N 350,514
Meta-analysisLarge GWAS
multi-ancestry
Allele A
OR 0.47
p 1.0e-9
N 312,296
Large GWAS
multi-ancestry

uric acid measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.02
p 5.0e-13
N 473,241
Large GWAS
multi-ancestry

urate measurement

Allele A
OR 0.02
p 5.0e-12
N 454,183
Meta-analysisLarge GWAS
European
Cho C et al. Large-scale cross-ancestry genome-wide meta-analysis of serum urate. Nature Communications 15(1):3441 (2024)
Allele A
OR 0.02
p 4.0e-10
N 677,373
Meta-analysisLarge GWAS
European
Allele A
OR 0.02
p 6.0e-12
N 394,642
Large GWAS
European

Research that mentions this SNP (1)

Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission
AssociationN=14,471Tonia C. Carter et al.(2018)· Journal of Medical Virology

This pilot screening study evaluated 32 SNPs in viral immune response genes for association with hospitalized seasonal influenza in adults of European ancestry using a discovery group (26 cases, 993 controls) and two validation groups (84 cases, 4,076 controls; 128 cases, 9,187 controls). The study failed to replicate the previously reported association between IFITM3 rs12252 and hospitalized influenza (P > 0.05), and a preliminary finding of association with SLFN13 rs8072510 (P = 0.0099 in discovery group) was not confirmed in validation groups.

Traits studied:Hospitalized seasonal influenzaInfluenza hospital admissionSevere influenza infection

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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